EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS044-10461 
Organism
Homo sapiens 
Tissue/cell
Fetal_kidney 
Coordinate
chr5:77799860-77802740 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs2277015chr577800588hg19
TF binding sites/motifs
Number: 8             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
CDX2MA0465.1chr5:77800496-77800507TTTTATTGCTT-6.32
NFAT5MA0606.1chr5:77801263-77801273AATGGAAAAT-6.02
NFATC1MA0624.1chr5:77801263-77801273AATGGAAAAT-6.02
NFATC3MA0625.1chr5:77801263-77801273AATGGAAAAT-6.02
RFX5MA0510.2chr5:77802209-77802225TGTTGCTCTGGCAACA+6.07
TFAP2CMA0524.2chr5:77800651-77800663AGCCCCAGGGCA+6.11
ZNF263MA0528.1chr5:77801288-77801309AGGGGAGGGGGAGGAAGGAGC+6.39
ZNF263MA0528.1chr5:77801282-77801303AGGGGAAGGGGAGGGGGAGGA+7.13
Number of super-enhancer constituents: 26             
IDCoordinateTissue/cell
SE_00744chr5:77799632-77801875Adipose_Nuclei
SE_01516chr5:77799767-77800303Adrenal_Gland
SE_01516chr5:77800328-77801493Adrenal_Gland
SE_02084chr5:77799778-77800837Aorta
SE_02084chr5:77800926-77801565Aorta
SE_02699chr5:77799902-77801516Astrocytes
SE_13177chr5:77799978-77800634CD34_Primary_RO01480
SE_13761chr5:77800385-77802849CD34_Primary_RO01536
SE_14327chr5:77801643-77802549CD34_Primary_RO01549
SE_25910chr5:77799563-77808605Duodenum_Smooth_Muscle
SE_29638chr5:77799474-77803204Fetal_Muscle
SE_36101chr5:77799462-77802446HMEC
SE_37067chr5:77799145-77808361HSMMtube
SE_38069chr5:77799675-77802027HUVEC
SE_44285chr5:77799521-77806899NHDF-Ad
SE_44858chr5:77799562-77803016NHLF
SE_45582chr5:77799364-77805037Osteoblasts
SE_51920chr5:77799864-77801500Skeletal_Muscle_Myoblast
SE_53244chr5:77799914-77802051Small_Intestine
SE_54871chr5:77799656-77803259Stomach_Smooth_Muscle
SE_55657chr5:77799733-77802979u87
SE_61959chr5:77778881-77810352Toledo
SE_63730chr5:77799657-77801514HSMM
SE_63730chr5:77801893-77802698HSMM
SE_64735chr5:77799668-77802009NHEK
SE_67593chr5:77799733-77802979u87
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr57780022577801516
Number: 1             
IDChromosomeStartEnd
GH05I078503chr57779962577808076
Enhancer Sequence
GGGACTACTA AAGGCTGATG AATTAGGAAA TGTGTCCTAT CAGTGGTATT TTAAAACTGA 60
TTCAGACACG GAACTGTTGG ACCTGACTTC TGGTGGAGCA TCATCTGTCT GGACAGCCAG 120
AAACCAAGAG CCTCCCTTTG GCAGCCAGAA GTCCTCAGGG CCTTGTGCTC ACCAGGAACA 180
AAAGGAAGGG CTGTTCCCTC TACTCTCCCC ATGCCTCTTT GAGGGTGTTC TGAAGGTGGG 240
CAACCAAGGT CACACCACCC CAGAGAAAGC CCGGTGACTT TTTCAGGAGA AAAATTCTGA 300
GGCAGGGCTC CATGTGTGCC AGGCATCTCC GTCCATCTCC CTATGCTTCC CAAGCCCCTG 360
TTCTGATTTC TCTCCTCTCA GTGGCTGACC TTGTCTTTTG GGCCTGAGAG TGAATGAGTA 420
GGGCATGAGA TCAGTCATGG GGTTGGGCTA TGGTCATAAC CTTGATGCTT AAGGTGATTT 480
TTTACCCTGT GTAAAAAGCA GTAAGAATAC CAAATCCTGG AGAGTGATCA GCTGCATTTC 540
GTATGCCCAC CCATACTTCC ATGCATCAGA TTTATGACAA AAGCAATTAT ATAAGCAGCA 600
AAGGCAAAAC CCCCACGTGT CTGTCTCTGC TTTTCCTTTT ATTGCTTTTT TTCATGTTGT 660
CCTCTTTCAC CCTCAATCAT TGCTCACTTC CAAGAAGGCT GAGCCTGCAT ACACCAGGCC 720
CTTCACCGCC ACTGCCAGCG CCATTCCCAC GACCACACAC CCTTCACCCC AGCCCTGCAG 780
AGGCAGGGTT CAGCCCCAGG GCAATCTATC TGGTCAGACT GGTGGGGCAG CTTGCTAAGG 840
CTGTCCTGCT GGACTGAGAC CCATGCAGGC AGAGGGCTGG AGGGAGTAGA GTGTGAGAGC 900
CAGCCCAGCA TAAAGGGAAG ACTGGAAGAT AGCAGGCAGC TGGCCGGTGG CTCATGCTTA 960
TGGCAGTCCC TGTGGAATAG GCCCAGCCAG CACAAGTGAG CCAAATCCTG AGCTCAGTTT 1020
AATGGCTTCG GTCCCAAACC TGAGTCACTG GGGATTCCAT GGACTTCTAA GAGAGCCCTA 1080
CACGCATTTC CAAAAACAAA CTGCTTGATG TTGTCATGGA AAACCTGGAT CTTTGCATTC 1140
TATGGTTTCA CGATGGATTA CATCCAGGTC ACAACCTAAG GAAGACAGCT GGCAAAAAGC 1200
CAACCCTGCT GGCTGATCAC CCGGCTTTTG TAATGAATCC CAGAGGGATG CAAACTGATG 1260
TGTGTTGCTG CCTCTGCCAA GTCCTTGGAC AAGTTCTCAC CTCATGAAGA CTAATCAACC 1320
TGTGATTTAC TCCGCCAGGA GAATCTCAGA AGCCACCTGC AATCAACACT CAACGGCTAG 1380
AAGCTGCCTC CAGAAAGAGA AGGAATGGAA AATGTGTGTG TCAGGGGAAG GGGAGGGGGA 1440
GGAAGGAGCT CTGTTTTCTT GTCAATTTGA CTGCTCTCTC CTGCCTTTTA AAAAAATGAT 1500
CTGAGGACAC CCCTGGTTAC ACCAAAGCCA CAGGACTGCT GTGCACCCTG AGCTCCAACA 1560
CAGGCAGGCT CTTAAGGACA GGGAAGGCCC CTACACACTG TATTTGTGTT TGATTGGAAC 1620
AGAGTAAGGT CAATTCTAAA AGCTACAAGA TATCCCTGTT CCGTAGAATG CAACAAATCC 1680
GGGAAACAAA TAATATACTA AAACTTGCCA AGAAAGCAGA AATACTTTGA TAATGATTCT 1740
ATAGCTACCA TTTATTATTT ACTGTGTGTT AAGCACTATG CTTAAGCCTT TCTCATATAT 1800
TATCTAACTT AATCCTCAGA ACAGTCCTGA GGTATAAACC TATTGTTATG CCCATTTTAC 1860
AAGTGAGAAA ACTATGGTTC AGAAAAGTGA GGCAAATTGG TCCGTGTTTC ACAGGCACAT 1920
TCAGGTGAGG CCTGAACCCT CATTACTGAG TGAGTGCTGA ATGTCAAGGA CATGTGCACA 1980
GTATTTAGAA AGTATCAGCC GGGTGTCCAC CTAATGGTGC CCTGAAGGCA GATCCTGCTA 2040
TCTGGATTCA CATAACAGGC AATGATTATA TTTCATTACT GCTTAAGTTA GCCCAGAGTT 2100
TGGGATTTCC ATTGAAGTAG CAGATTCTTT CACACCCAGT TTCTAAACTC AGAATATCAA 2160
GATTTTGATT ATTTATGCTG TGTTTTTTTA TAGACAGTGA AGGCTACACA AGCCTGTGGC 2220
CTATTTATAT CTTAAAATTA GGTGTAGCAA AAGAATATGC TTACGATCAT TTCTCATCCA 2280
GTCACATTTT TGCCAAAATG TAAGTTGTAA GAACAAACAC AGCCTGAGTG TATTTCTAAA 2340
GAATCCTTTT GTTGCTCTGG CAACAGCCTC CTTTCTCACC ATTTGTTTCA GTGTTGAAGA 2400
GATCCAGGGC TGAGGGAGAG GGGGCATAGG GAGAGAAAAG GCAGATGCTC CCAGCTGCAG 2460
CAAGTCCTTG CTGAGGCTGG GGCTGACCAG AGGCTATCAC AGATTGGCCA ACGGGAGAAA 2520
GCAAGCCAGC CCTTTCAGAT GCCAGTATGG CAATGTCCTC AGCCACAGAT TCAAGAACCA 2580
CAGCTGCCCT TTACATTGGC TTGATGTGCA TGATGAGACC TCCAATAGGG GAGAAAGTGC 2640
CCACTGAATC ATGAGAAGGA TAGCTCAGTC CCTCTTTTTT ATGATTTTTT CTCTGAGGGG 2700
TGATGCTAGG CTGGAAGGAG AAAAGAAACC AGTTCTTTCC TGTATTTCAG CACTTAGTCT 2760
TAGATCAGTG GCTCCTAGAC AGCAGTCAAA CTATGCAGGA ATCTCTGCCT TGTGCCAATT 2820
TAAAATTCTG AGTAATTTCA GAATTTTTGA GATGCTGCAT AAGTAACAGG GGTAGGGAGG 2880